chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89110954	89110955	G	GT	3	INTERGENIC	heterozygous	51997384
10	89112058	89112059	A	AG	4	INTERGENIC	homozygous	51536545
10	89112346	89112347	C	T	6	INTERGENIC	heterozygous	51731661
10	89116847	89116851	CCCT	----	9	GENIC	heterozygous	51731716
10	89128334	89128335	T	C	25	GENIC	homozygous	51536557
10	89131500	89131501	G	T	12	GENIC	possibly homozygous	51536561
10	89131731	89131732	A	T	24	GENIC	possibly homozygous	51536562
10	89131898	89131899	A	G	9	GENIC	homozygous	51731818
10	89132027	89132028	C	T	4	GENIC	homozygous	51925367
10	89132048	89132049	C	CA	3	GENIC	homozygous	51925369
10	89132049	89132050	C	A	3	GENIC	homozygous	52394334
10	89132315	89132316	A	G	7	GENIC	homozygous	51925373
10	89132537	89132538	C	T	4	GENIC	homozygous	51536566
10	89132753	89132754	G	A	30	GENIC	possibly homozygous	51925375
10	89132838	89132839	A	G	8	GENIC	homozygous	51536567
10	89133579	89133580	A	G	16	GENIC	possibly homozygous	51536572
10	89133913	89133914	T	C	5	GENIC	homozygous	51536574
10	89134105	89134106	A	T	6	GENIC	heterozygous	51536575
10	89134601	89134602	T	C	1	GENIC	homozygous	51536581
10	89134606	89134619	TTTTCTTTTCTTT	-------------	1	GENIC	homozygous	52394338
10	89134938	89134939	A	C	21	GENIC	homozygous	51536585
10	89135109	89135110	C	T	7	GENIC	possibly homozygous	51925379
10	89135381	89135382	C	T	4	GENIC	heterozygous	51536591
10	89135494	89135495	C	A	9	GENIC	heterozygous	51536592
10	89135732	89135733	T	C	16	GENIC	possibly homozygous	51536593
10	89136078	89136079	T	G	5	GENIC	homozygous	51536594
10	89136695	89136696	T	C	2	INTERGENIC	homozygous	51536595
10	89136703	89136704	A	ATCTGC	2	INTERGENIC	homozygous	51536596
10	89136819	89136820	T	C	11	INTERGENIC	homozygous	51536597
10	89136824	89136825	T	C	11	INTERGENIC	possibly homozygous	51536598
10	89139927	89139928	A	G	14	GENIC	homozygous	51731830